Thomsen Rune, Libri Domenico, Boulay Jocelyne, Rosbash Michael, Jensen Torben Heick
Department of Molecular Biology, Aarhus University, 8000 Aarhus C., Denmark.
RNA. 2003 Sep;9(9):1049-57. doi: 10.1261/rna.5170303.
In the yeast Saccharomyces cerevisiae, a common conditional phenotype associated with deletion or mutation of genes encoding mRNA export factors is the rapid accumulation of mRNAs in intranuclear foci, suggested to be near transcription sites. The nuclear RNA exosome has been implicated in retaining RNAs in these foci; on deletion of the exosome component Rrp6p, the RNA is released. To determine the exact nuclear location of retained as well as released mRNAs, we have used mRNA export mutant strains to analyze the spatial relationship between newly synthesized heat shock mRNA, the chromosomal site of transcription, and known S. cerevisiae nuclear structures such as the nucleolus and the nucleolar body. Our results show that retained SSA4 RNA localizes to an area in close proximity to the SSA4 locus. On deletion of Rrp6p and release from the genomic locus, heat shock mRNAs produced in the rat7-1 strain colocalize predominantly with nucleolar antigens. Bulk poly(A)(+) RNA, on the other hand, is localized primarily to the nuclear rim. Interestingly, the RNA binding nucleocytoplasmic shuttle protein Npl3p shows strong colocalization with bulk poly(A)(+) RNA, regardless of its nuclear location. Taken together, our data show that retention occurs close to the gene and indicate distinct nuclear fates of different mRNAs.
在酿酒酵母中,与编码mRNA输出因子的基因缺失或突变相关的一种常见条件表型是mRNA在核内聚集体中快速积累,这些聚集体被认为靠近转录位点。核RNA外切体被认为与RNA在这些聚集体中的保留有关;外切体组分Rrp6p缺失时,RNA会被释放。为了确定保留的和释放的mRNA的确切核定位,我们使用mRNA输出突变菌株来分析新合成的热休克mRNA、转录染色体位点以及酿酒酵母已知的核结构(如核仁与核仁体)之间的空间关系。我们的结果表明,保留的SSA4 RNA定位于与SSA4基因座紧邻的区域。在Rrp6p缺失并从基因组位点释放后,在rat7 - 1菌株中产生的热休克mRNA主要与核仁抗原共定位。另一方面,大量的聚腺苷酸(poly(A))RNA主要定位于核边缘。有趣的是,RNA结合核质穿梭蛋白Npl3p与大量的聚腺苷酸(poly(A))RNA表现出强烈的共定位,无论其在核内的位置如何。综合来看,我们的数据表明RNA保留发生在基因附近,并表明不同mRNA在核内有不同的命运。